Canonical Allele Identifier: CA571116580

Gene:

Linked Data

• dbSNP Id: rs1461610652
• gnomAD v2: 6-151954921-T-C
• gnomAD v3: 6-151633786-T-C
• gnomAD v4: 6-151633786-T-C
• MyVariant Identifiers: chr6:g.151954921T>C (hg19) ; chr6:g.151633786T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633786T>C , CM000668.2:g.151633786T>C	GRCh38
NC_000006.11:g.151954921T>C , CM000668.1:g.151954921T>C	GRCh37
NC_000006.10:g.151996614T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943115.1:n.2496+3804T>C