Canonical Allele Identifier: CA836922001

Gene:

Linked Data

• dbSNP Id: rs990339083
• gnomAD v3: 7-24283584-G-A
• gnomAD v4: 7-24283584-G-A
• MyVariant Identifiers: chr7:g.24323203G>A (hg19) ; chr7:g.24283584G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283584G>A , CM000669.2:g.24283584G>A	GRCh38
NC_000007.13:g.24323203G>A , CM000669.1:g.24323203G>A	GRCh37
NC_000007.12:g.24289728G>A	NCBI36
NG_016148.1:g.4397G>A

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-27885C>T	XP_016868399.1:n.42-27885C>T
XM_017012911.1:c.42-27885C>T	XP_016868400.1:n.42-27885C>T
XR_001745121.1:n.473+35773C>T
XR_001745122.1:n.345-86555C>T
XR_001745123.1:n.473+35773C>T
XR_001745124.1:n.473+35773C>T
XR_001745125.1:n.473+35773C>T
XR_001745126.1:n.473+35773C>T
XR_001745127.1:n.345-27885C>T
XR_001745129.1:n.473+35773C>T
XR_001745130.1:n.473+35773C>T
XR_001745131.1:n.473+35773C>T
XR_001745132.1:n.473+35773C>T