Canonical Allele Identifier: CA150690510

Gene:

Linked Data

• dbSNP Id: rs1002040890
• COSMIC: COSN6310239
• MyVariant Identifiers: chr6:g.156133721T>C (hg19) ; chr6:g.155812587T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812587T>C , CM000668.2:g.155812587T>C	GRCh38
NC_000006.11:g.156133721T>C , CM000668.1:g.156133721T>C	GRCh37
NC_000006.10:g.156175413T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19168T>C
XR_943146.1:n.645-548A>G
XR_001744423.1:n.699-548A>G
XR_001744424.1:n.79+19168T>C