Canonical Allele Identifier: CA1127875722

Gene:

Linked Data

• dbSNP Id: rs1587835283
• gnomAD v3: 9-108092995-G-T
• gnomAD v4: 9-108092995-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108092995G>T , CM000671.2:g.108092995G>T	GRCh38
NC_000009.11:g.110855276G>T , CM000671.1:g.110855276G>T	GRCh37
NC_000009.10:g.109895097G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930239.1:n.461-39701C>A
XR_001746881.1:n.668-39701C>A
XR_001746882.1:n.668-39701C>A