Linked Data
ClinVar Variation Id:
3001472
ClinVar RCV Id:
RCV003852615
gnomAD v4:
7-128986795-G-A
MyVariant Identifiers:
chr7:g.128626849G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128986795G>A , CM000669.2:g.128986795G>A | GRCh38 |
| NC_000007.13:g.128626849G>A , CM000669.1:g.128626849G>A | GRCh37 |
| NC_000007.12:g.128414085G>A | NCBI36 |
| NG_023428.1:g.73379C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265388.10:c.1624C>T MANE Select | ENSP00000265388.5:p.Leu542= | |
| ENST00000265388.9:c.1624C>T | ENSP00000265388.5:p.Leu542= | |
| ENST00000471166.1:c.1726C>T | ENSP00000418267.1:p.Leu576= | |
| ENST00000471234.5:c.1499-2536C>T | ENSP00000418646.1:n.1499-2536C>T | |
| ENST00000482320.5:c.1426C>T | ENSP00000420089.1:p.Leu476= | |
| ENST00000627585.2:c.1726C>T | ENSP00000487231.1:p.Leu576= | |
| NM_001191028.2:c.1499-2536C>T | NP_001177957.2:n.1499-2536C>T | |
| NM_012470.3:c.1624C>T | NP_036602.1:p.Leu542= | |
| NR_034053.2:n.2188C>T | ||
| XM_011515989.1:c.1426C>T | XP_011514291.1:p.Leu476= | |
| NM_001191028.3:c.1499-2536C>T | NP_001177957.2:n.1499-2536C>T | |
| NM_001382216.1:c.1726C>T | NP_001369145.1:p.Leu576= | |
| NM_001382217.1:c.1705C>T | NP_001369146.1:p.Leu569= | |
| NM_001382218.1:c.1624C>T | NP_001369147.1:p.Leu542= | |
| NM_001382219.1:c.1516C>T | NP_001369148.1:p.Leu506= | |
| NM_001382220.1:c.1624C>T | NP_001369149.1:p.Leu542= | |
| NM_001382221.1:c.1480C>T | NP_001369150.1:p.Leu494= | |
| NM_001382222.1:c.1477C>T | NP_001369151.1:p.Leu493= | |
| NM_001382223.1:c.1499-2536C>T | NP_001369152.1:n.1499-2536C>T | |
| NM_012470.4:c.1624C>T MANE Select | NP_036602.1:p.Leu542= | |
| NR_034053.3:n.2126C>T | ||
| NR_167911.1:n.2213C>T | ||
| NR_167912.1:n.1965C>T | ||
| NR_167913.1:n.1873C>T | ||
| NR_167914.1:n.2033C>T | ||
| NR_167915.1:n.2126C>T | ||
| NR_167916.1:n.1965C>T | ||
| NR_167917.1:n.1873C>T | ||
| NR_167918.1:n.2251C>T | ||
| NR_167919.1:n.2090C>T | ||
| NR_167920.1:n.2251C>T | ||
| NR_167921.1:n.2251C>T | ||
| NR_167922.1:n.2087C>T | ||
| NR_167923.1:n.2090C>T | ||
| NR_167924.1:n.1965C>T | ||
| NR_167925.1:n.1965C>T | ||
| NR_167926.1:n.2101C>T | ||
| NR_167927.1:n.2192C>T |