Canonical Allele Identifier: CA150162962

Gene:

Linked Data

• dbSNP Id: rs962139916
• gnomAD v2: 6-151954824-T-G
• gnomAD v3: 6-151633689-T-G
• gnomAD v4: 6-151633689-T-G
• MyVariant Identifiers: chr6:g.151954824T>G (hg19) ; chr6:g.151633689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633689T>G , CM000668.2:g.151633689T>G	GRCh38
NC_000006.11:g.151954824T>G , CM000668.1:g.151954824T>G	GRCh37
NC_000006.10:g.151996517T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3707T>G