Canonical Allele Identifier: CA155828793

Gene:

Linked Data

• dbSNP Id: rs918693300
• gnomAD v2: 7-24322971-T-A
• gnomAD v3: 7-24283352-T-A
• gnomAD v4: 7-24283352-T-A
• MyVariant Identifiers: chr7:g.24322971T>A (hg19) ; chr7:g.24283352T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283352T>A , CM000669.2:g.24283352T>A	GRCh38
NC_000007.13:g.24322971T>A , CM000669.1:g.24322971T>A	GRCh37
NC_000007.12:g.24289496T>A	NCBI36
NG_016148.1:g.4165T>A

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27653A>T	XP_016868399.1:n.42-27653A>T
XM_017012911.1:c.42-27653A>T	XP_016868400.1:n.42-27653A>T
XR_001745121.1:n.473+36005A>T
XR_001745122.1:n.345-86323A>T
XR_001745123.1:n.473+36005A>T
XR_001745124.1:n.473+36005A>T
XR_001745125.1:n.473+36005A>T
XR_001745126.1:n.473+36005A>T
XR_001745127.1:n.345-27653A>T
XR_001745129.1:n.473+36005A>T
XR_001745130.1:n.473+36005A>T
XR_001745131.1:n.473+36005A>T
XR_001745132.1:n.473+36005A>T