Canonical Allele Identifier: CA571581147

Gene:

Linked Data

• dbSNP Id: rs1375205469
• gnomAD v2: 6-156133781-G-C
• gnomAD v3: 6-155812647-G-C
• gnomAD v4: 6-155812647-G-C
• MyVariant Identifiers: chr6:g.156133781G>C (hg19) ; chr6:g.155812647G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812647G>C , CM000668.2:g.155812647G>C	GRCh38
NC_000006.11:g.156133781G>C , CM000668.1:g.156133781G>C	GRCh37
NC_000006.10:g.156175473G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19228G>C
XR_943146.1:n.645-608C>G
XR_001744423.1:n.699-608C>G
XR_001744424.1:n.79+19228G>C