Canonical Allele Identifier: CA1694877515

Gene:

Linked Data

• dbSNP Id: rs1787632921
• gnomAD v4: 7-24291889-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291889T>C , CM000669.2:g.24291889T>C	GRCh38
NC_000007.13:g.24331508T>C , CM000669.1:g.24331508T>C	GRCh37
NC_000007.12:g.24298033T>C	NCBI36
NG_016148.1:g.12702T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.41+27468A>G	XP_016868399.1:n.41+27468A>G
XM_017012911.1:c.41+27468A>G	XP_016868400.1:n.41+27468A>G
XR_001745121.1:n.473+27468A>G
XR_001745122.1:n.345-94860A>G
XR_001745123.1:n.473+27468A>G
XR_001745124.1:n.473+27468A>G
XR_001745125.1:n.473+27468A>G
XR_001745126.1:n.473+27468A>G
XR_001745127.1:n.345-36190A>G
XR_001745129.1:n.473+27468A>G
XR_001745130.1:n.473+27468A>G
XR_001745131.1:n.473+27468A>G
XR_001745132.1:n.473+27468A>G