Canonical Allele Identifier: CA571581143

Gene:

Linked Data

• dbSNP Id: rs1432868864
• gnomAD v2: 6-156133751-T-G
• gnomAD v3: 6-155812617-T-G
• gnomAD v4: 6-155812617-T-G
• MyVariant Identifiers: chr6:g.156133751T>G (hg19) ; chr6:g.155812617T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812617T>G , CM000668.2:g.155812617T>G	GRCh38
NC_000006.11:g.156133751T>G , CM000668.1:g.156133751T>G	GRCh37
NC_000006.10:g.156175443T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19198T>G
XR_943146.1:n.645-578A>C
XR_001744423.1:n.699-578A>C
XR_001744424.1:n.79+19198T>G