Canonical Allele Identifier: CA821223656

Gene:

Linked Data

• dbSNP Id: rs1299005091
• gnomAD v3: 6-155812610-G-T
• gnomAD v4: 6-155812610-G-T
• MyVariant Identifiers: chr6:g.156133744G>T (hg19) ; chr6:g.155812610G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812610G>T , CM000668.2:g.155812610G>T	GRCh38
NC_000006.11:g.156133744G>T , CM000668.1:g.156133744G>T	GRCh37
NC_000006.10:g.156175436G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19191G>T
XR_943146.1:n.645-571C>A
XR_001744423.1:n.699-571C>A
XR_001744424.1:n.79+19191G>T