Canonical Allele Identifier: CA836922038

Gene:

Linked Data

• dbSNP Id: rs1216300919
• gnomAD v3: 7-24283610-C-T
• gnomAD v4: 7-24283610-C-T
• MyVariant Identifiers: chr7:g.24323229C>T (hg19) ; chr7:g.24283610C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283610C>T , CM000669.2:g.24283610C>T	GRCh38
NC_000007.13:g.24323229C>T , CM000669.1:g.24323229C>T	GRCh37
NC_000007.12:g.24289754C>T	NCBI36
NG_016148.1:g.4423C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27911G>A	XP_016868399.1:n.42-27911G>A
XM_017012911.1:c.42-27911G>A	XP_016868400.1:n.42-27911G>A
XR_001745121.1:n.473+35747G>A
XR_001745122.1:n.345-86581G>A
XR_001745123.1:n.473+35747G>A
XR_001745124.1:n.473+35747G>A
XR_001745125.1:n.473+35747G>A
XR_001745126.1:n.473+35747G>A
XR_001745127.1:n.345-27911G>A
XR_001745129.1:n.473+35747G>A
XR_001745130.1:n.473+35747G>A
XR_001745131.1:n.473+35747G>A
XR_001745132.1:n.473+35747G>A