Linked Data
dbSNP Id:
rs772113749
gnomAD v3:
4-6301457-G-C
gnomAD v4:
4-6301457-G-C
MyVariant Identifiers:
chr4:g.6303184G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6301457G>C , CM000666.2:g.6301457G>C | GRCh38 |
| NC_000004.11:g.6303184G>C , CM000666.1:g.6303184G>C | GRCh37 |
| NC_000004.10:g.6354085G>C | NCBI36 |
| NG_011700.1:g.36608G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.1698G>C | ENSP00000507852.1:p.Leu566= | |
| ENST00000683395.1:c.1639G>C | ||
| ENST00000684087.1:c.1662G>C | ENSP00000506978.1:p.Leu554= | |
| ENST00000506362.2:c.1413G>C | ENSP00000424103.2:p.Leu471= | |
| ENST00000673642.1:c.1321G>C | ENSP00000501242.1:n.1321G>C | |
| ENST00000673991.1:c.1698G>C | ENSP00000501033.1:p.Leu566= | |
| ENST00000226760.5:c.1662G>C MANE Select | ENSP00000226760.1:p.Leu554= | |
| ENST00000503569.5:c.1662G>C | ENSP00000423337.1:p.Leu554= | |
| ENST00000507765.1:n.1847G>C | ||
| NM_001145853.1:c.1662G>C | NP_001139325.1:p.Leu554= | |
| NM_006005.3:c.1662G>C MANE Select | NP_005996.2:p.Leu554= | |
| XM_017008586.1:c.1671G>C | XP_016864075.1:p.Leu557= |