Canonical Allele Identifier: CA93117876

Gene:

Linked Data

• dbSNP Id: rs915758513
• MyVariant Identifiers: chr4:g.12579602G>T (hg19) ; chr4:g.12577978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12577978G>T , CM000666.2:g.12577978G>T	GRCh38
NC_000004.11:g.12579602G>T , CM000666.1:g.12579602G>T	GRCh37
NC_000004.10:g.12188700G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925406.1:n.106+31364C>A
XR_001741374.1:n.254+44677C>A
XR_925406.3:n.140+31364C>A