Canonical Allele Identifier: CA571581102

Gene:

Linked Data

• dbSNP Id: rs1363340469
• gnomAD v2: 6-156133572-T-C
• gnomAD v3: 6-155812438-T-C
• gnomAD v4: 6-155812438-T-C
• MyVariant Identifiers: chr6:g.156133572T>C (hg19) ; chr6:g.155812438T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812438T>C , CM000668.2:g.155812438T>C	GRCh38
NC_000006.11:g.156133572T>C , CM000668.1:g.156133572T>C	GRCh37
NC_000006.10:g.156175264T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19019T>C
XR_943146.1:n.645-399A>G
XR_001744423.1:n.699-399A>G
XR_001744424.1:n.79+19019T>C