Canonical Allele Identifier: CA150691053

Gene:

Linked Data

• dbSNP Id: rs529511622
• gnomAD v2: 6-156138783-T-C
• gnomAD v3: 6-155817649-T-C
• gnomAD v4: 6-155817649-T-C
• MyVariant Identifiers: chr6:g.156138783T>C (hg19) ; chr6:g.155817649T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155817649T>C , CM000668.2:g.155817649T>C	GRCh38
NC_000006.11:g.156138783T>C , CM000668.1:g.156138783T>C	GRCh37
NC_000006.10:g.156180475T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943142.1:n.79+24230T>C
XR_943146.1:n.552-2979A>G
XR_001744423.1:n.606-2979A>G
XR_001744424.1:n.79+24230T>C