Canonical Allele Identifier: CA786695540

Gene:

Linked Data

• dbSNP Id: rs1167567518
• gnomAD v3: 4-12578186-T-A
• gnomAD v4: 4-12578186-T-A
• MyVariant Identifiers: chr4:g.12579810T>A (hg19) ; chr4:g.12578186T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12578186T>A , CM000666.2:g.12578186T>A	GRCh38
NC_000004.11:g.12579810T>A , CM000666.1:g.12579810T>A	GRCh37
NC_000004.10:g.12188908T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_925406.1:n.106+31156A>T
XR_001741374.1:n.254+44469A>T
XR_925406.3:n.140+31156A>T