Canonical Allele Identifier: CA814334973

Gene:

Linked Data

• dbSNP Id: rs1443195974
• gnomAD v3: 5-79549796-C-T
• gnomAD v4: 5-79549796-C-T
• MyVariant Identifiers: chr5:g.78845619C>T (hg19) ; chr5:g.79549796C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79549796C>T , CM000667.2:g.79549796C>T	GRCh38
NC_000005.9:g.78845619C>T , CM000667.1:g.78845619C>T	GRCh37
NC_000005.8:g.78881375C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948497.1:n.72+2152C>T
XR_948498.1:n.159+1959C>T
XR_948499.1:n.67+1494C>T
XR_948497.2:n.72+2152C>T
XR_948498.2:n.159+1959C>T
XR_948499.2:n.225+1494C>T