Canonical Allele Identifier: CA150162834

Gene:

Linked Data

• dbSNP Id: rs11753383
• MyVariant Identifiers: chr6:g.151954659G>C (hg19) ; chr6:g.151633524G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633524G>C , CM000668.2:g.151633524G>C	GRCh38
NC_000006.11:g.151954659G>C , CM000668.1:g.151954659G>C	GRCh37
NC_000006.10:g.151996352G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3542G>C