Canonical Allele Identifier: CA1929213308
Gene:

Linked Data

dbSNP Id: rs1564656803
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762498G>A , CM000672.2:g.94762498G>A GRCh38
NC_000010.10:g.96522255G>A , CM000672.1:g.96522255G>A GRCh37
NC_000010.9:g.96512245G>A NCBI36
NG_008384.2:g.4793G>A
NG_008384.3:g.4818G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12560G>A ENSP00000483243.1:n.932-12560G>A
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