Canonical Allele Identifier: CA1458504733
Gene:

Linked Data

dbSNP Id: rs1720478658
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228388C>A , CM000666.2:g.54228388C>A GRCh38
NC_000004.11:g.55094555C>A , CM000666.1:g.55094555C>A GRCh37
NC_000004.10:g.54789312C>A NCBI36
NG_009250.1:g.4292C>A , LRG_309:g.4292C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46537C>A ENSP00000423325.1:n.1018-46537C>A
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