Canonical Allele Identifier: CA155828717

Gene:

Linked Data

• dbSNP Id: rs970664692
• MyVariant Identifiers: chr7:g.24322314G>C (hg19) ; chr7:g.24282695G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24282695G>C , CM000669.2:g.24282695G>C	GRCh38
NC_000007.13:g.24322314G>C , CM000669.1:g.24322314G>C	GRCh37
NC_000007.12:g.24288839G>C	NCBI36
NG_016148.1:g.3508G>C

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-26996C>G	XP_016868399.1:n.42-26996C>G
XM_017012911.1:c.42-26996C>G	XP_016868400.1:n.42-26996C>G
XR_001745121.1:n.473+36662C>G
XR_001745122.1:n.345-85666C>G
XR_001745123.1:n.473+36662C>G
XR_001745124.1:n.473+36662C>G
XR_001745125.1:n.473+36662C>G
XR_001745126.1:n.473+36662C>G
XR_001745127.1:n.345-26996C>G
XR_001745129.1:n.473+36662C>G
XR_001745130.1:n.473+36662C>G
XR_001745131.1:n.473+36662C>G
XR_001745132.1:n.473+36662C>G