Canonical Allele Identifier: CA571116558

Gene:

Linked Data

• dbSNP Id: rs1210708744
• gnomAD v2: 6-151954793-A-C
• gnomAD v3: 6-151633658-A-C
• gnomAD v4: 6-151633658-A-C
• MyVariant Identifiers: chr6:g.151954793A>C (hg19) ; chr6:g.151633658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633658A>C , CM000668.2:g.151633658A>C	GRCh38
NC_000006.11:g.151954793A>C , CM000668.1:g.151954793A>C	GRCh37
NC_000006.10:g.151996486A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3676A>C