Canonical Allele Identifier: CA1096188062

Gene:

Linked Data

• dbSNP Id: rs1778855214
• gnomAD v3: 6-155812404-C-T
• gnomAD v4: 6-155812404-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812404C>T , CM000668.2:g.155812404C>T	GRCh38
NC_000006.11:g.156133538C>T , CM000668.1:g.156133538C>T	GRCh37
NC_000006.10:g.156175230C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+18985C>T
XR_943146.1:n.645-365G>A
XR_001744423.1:n.699-365G>A
XR_001744424.1:n.79+18985C>T