Canonical Allele Identifier: CA145511534

Gene:

Linked Data

• dbSNP Id: rs752086960
• gnomAD v2: 6-106253121-G-A
• gnomAD v3: 6-105805246-G-A
• gnomAD v4: 6-105805246-G-A
• MyVariant Identifiers: chr6:g.106253121G>A (hg19) ; chr6:g.105805246G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.105805246G>A , CM000668.2:g.105805246G>A	GRCh38
NC_000006.11:g.106253121G>A , CM000668.1:g.106253121G>A	GRCh37
NC_000006.10:g.106359814G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942835.1:n.510+24811C>T
XR_001744274.1:n.438+24811C>T
XR_001744275.1:n.337+24811C>T