Linked Data
dbSNP Id:
rs1221639671
gnomAD v2:
9-99006572-C-G
gnomAD v3:
9-96244290-C-G
gnomAD v4:
9-96244290-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.96244290C>G , CM000671.2:g.96244290C>G | GRCh38 |
| NC_000009.11:g.99006572C>G , CM000671.1:g.99006572C>G | GRCh37 |
| NC_000009.10:g.98046393C>G | NCBI36 |
| NG_008157.1:g.62863G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375262.4:c.672+39G>C | ENSP00000364411.2:n.672+39G>C | |
| ENST00000375263.8:c.672+39G>C MANE Select | ENSP00000364412.3:n.672+39G>C | |
| ENST00000463517.2:n.2214+39G>C | ||
| ENST00000464104.6:n.1610+39G>C | ||
| ENST00000467499.6:c.*371+39G>C | ENSP00000498077.1:n.*371+39G>C | |
| ENST00000484816.2:n.23+39G>C | ||
| ENST00000494814.6:n.222+1G>C | ||
| ENST00000643789.1:c.2964+39G>C | ||
| ENST00000648146.1:c.672+39G>C | ENSP00000497238.1:n.672+39G>C | |
| ENST00000648332.1:c.349+39G>C | ENSP00000497562.1:n.349+39G>C | |
| ENST00000648799.1:c.564+39G>C | ENSP00000498039.1:n.564+39G>C | |
| ENST00000650005.1:c.601+39G>C | ENSP00000498121.1:n.601+39G>C | |
| ENST00000375262.3:c.672+39G>C | ENSP00000364411.2:n.672+39G>C | |
| ENST00000375263.7:c.672+39G>C | ENSP00000364412.3:n.672+39G>C | |
| ENST00000464104.5:n.525+39G>C | ||
| ENST00000484816.1:n.22+39G>C | ||
| ENST00000494814.5:n.231+1G>C | ||
| NM_000197.1:c.672+39G>C | NP_000188.1:n.672+39G>C | |
| XM_005251970.3:c.312+39G>C | XP_005252027.1:n.312+39G>C | |
| XM_011518618.1:c.672+39G>C | XP_011516920.1:n.672+39G>C | |
| XM_011518619.1:c.672+39G>C | XP_011516921.1:n.672+39G>C | |
| XM_011518620.1:c.564+39G>C | XP_011516922.1:n.564+39G>C | |
| XM_011518621.1:c.710+1G>C | XP_011516923.1:n.710+1G>C | |
| NM_000197.2:c.672+39G>C MANE Select | NP_000188.1:n.672+39G>C | |
| XM_011518618.2:c.672+39G>C | XP_011516920.1:n.672+39G>C | |
| XM_011518619.2:c.672+39G>C | XP_011516921.1:n.672+39G>C | |
| XM_017014671.1:c.672+39G>C | XP_016870160.1:n.672+39G>C | |
| XM_017014672.1:c.672+39G>C | XP_016870161.1:n.672+39G>C | |
| XM_017014673.2:c.636+39G>C | XP_016870162.1:n.636+39G>C | |
| XM_017014674.1:c.564+39G>C | XP_016870163.1:n.564+39G>C | |
| XM_017014675.1:c.510+39G>C | XP_016870164.1:n.510+39G>C | |
| XM_017014677.1:c.312+39G>C | XP_016870166.1:n.312+39G>C | |
| XM_024447529.1:c.510+39G>C | XP_024303297.1:n.510+39G>C | |
| XR_002956778.1:n.3144+1G>C |