Canonical Allele Identifier: CA1581765828
Gene:

Linked Data

dbSNP Id: rs1758560290
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386951C>A , CM000667.2:g.129386951C>A GRCh38
NC_000005.9:g.128722644C>A , CM000667.1:g.128722644C>A GRCh37
NC_000005.8:g.128750543C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427770.2:n.163-1497C>A
XR_948774.1:n.235-5700C>A
XR_001742463.1:n.4089-1497C>A
XR_001742464.1:n.2019-5700C>A
XR_001742465.1:n.401-1497C>A
XR_427770.3:n.337-1497C>A
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