Linked Data
dbSNP Id:
rs764210072
gnomAD v4:
6-157148868-G-T
MyVariant Identifiers:
chr6:g.157470002G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.157148868G>T , CM000668.2:g.157148868G>T | GRCh38 |
| NC_000006.11:g.157470002G>T , CM000668.1:g.157470002G>T | GRCh37 |
| NC_000006.10:g.157511694G>T | NCBI36 |
| NG_032093.1:g.375939G>T | |
| NG_032093.2:g.375939G>T | |
| NG_066624.1:g.377843G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350026.11:c.3006G>T | ENSP00000055163.8:p.Gly1002= | |
| ENST00000414678.8:c.2916G>T | ENSP00000412835.3:p.Gly972= | |
| ENST00000637015.2:c.3006G>T | ENSP00000489729.2:p.Gly1002= | |
| ENST00000319584.11:c.1020G>T | ENSP00000313006.7:p.Gly340= | |
| ENST00000346085.10:c.3045G>T | ENSP00000344546.5:p.Gly1015= | |
| ENST00000350026.10:c.2757G>T | ENSP00000055163.7:p.Gly919= | |
| ENST00000414678.7:c.1164G>T | ENSP00000412835.2:p.Gly388= | |
| ENST00000452544.2:n.907G>T | ||
| ENST00000635849.1:c.327G>T | ENSP00000490948.1:p.Gly109= | |
| ENST00000636426.1:n.140G>T | ||
| ENST00000636930.2:c.3006G>T MANE Select | ENSP00000490491.2:p.Gly1002= | |
| ENST00000637015.1:c.245G>T | ||
| ENST00000637568.1:c.49G>T | ||
| ENST00000637810.1:c.507G>T | ENSP00000489636.1:p.Gly169= | |
| ENST00000637904.1:c.507G>T | ENSP00000490550.1:p.Gly169= | |
| ENST00000647938.1:c.2796G>T | ENSP00000498155.1:p.Gly932= | |
| ENST00000674190.1:n.1755G>T | ||
| ENST00000319584.10:c.1023G>T | ENSP00000313006.6:p.Gly341= | |
| ENST00000346085.9:c.2796G>T | ENSP00000344546.4:p.Gly932= | |
| ENST00000350026.9:c.2757G>T | ENSP00000055163.7:p.Gly919= | |
| ENST00000414678.6:c.1164G>T | ENSP00000412835.2:p.Gly388= | |
| ENST00000452544.1:n.853G>T | ||
| ENST00000478761.3:c.79G>T | ||
| NM_017519.2:c.2757G>T | NP_059989.2:p.Gly919= | |
| NM_020732.3:c.2796G>T | NP_065783.3:p.Gly932= | |
| XM_005267069.3:c.2757G>T | XP_005267126.2:p.Gly919= | |
| XM_011535984.1:c.1707G>T | XP_011534286.1:p.Gly569= | |
| XM_011535985.1:c.1527G>T | XP_011534287.1:p.Gly509= | |
| XM_011535986.1:c.1287G>T | XP_011534288.1:p.Gly429= | |
| XM_011535987.1:c.906G>T | XP_011534289.1:p.Gly302= | |
| XM_011535988.1:c.-20+15661G>T | XP_011534290.1:n.-20+15661G>T | |
| NM_001346813.1:c.2757G>T | NP_001333742.1:p.Gly919= | |
| NM_001363725.1:c.507G>T | NP_001350654.1:p.Gly169= | |
| XM_011535984.2:c.2838G>T | XP_011534286.2:p.Gly946= | |
| XM_011535988.3:c.-20+15661G>T | XP_011534290.1:n.-20+15661G>T | |
| XM_017011103.2:c.2838G>T | XP_016866592.1:p.Gly946= | |
| XM_017011104.1:c.2838G>T | XP_016866593.1:p.Gly946= | |
| XM_017011105.2:c.2838G>T | XP_016866594.1:p.Gly946= | |
| XM_017011106.2:c.2838G>T | XP_016866595.1:p.Gly946= | |
| XM_017011107.2:c.2658G>T | XP_016866596.1:p.Gly886= | |
| XR_002956289.1:n.2921G>T | ||
| NM_001363725.2:c.507G>T | NP_001350654.1:p.Gly169= | |
| NM_001371656.1:c.3045G>T | NP_001358585.1:p.Gly1015= | |
| NM_001374820.1:c.3045G>T | NP_001361749.1:p.Gly1015= | |
| NM_001374828.1:c.3006G>T MANE Select | NP_001361757.1:p.Gly1002= | |
| NM_017519.3:c.3006G>T | NP_059989.3:p.Gly1002= |