Canonical Allele Identifier: CA150159475

Gene:

Linked Data

• dbSNP Id: rs796422958
• gnomAD v4: 6-151627292-G-C
• MyVariant Identifiers: chr6:g.151948427G>C (hg19) ; chr6:g.151627292G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627292G>C , CM000668.2:g.151627292G>C	GRCh38
NC_000006.11:g.151948427G>C , CM000668.1:g.151948427G>C	GRCh37
NC_000006.10:g.151990120G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.718G>C
XR_943115.1:n.718G>C