Canonical Allele Identifier: CA2055289485
Gene:

Linked Data

dbSNP Id: rs1202578011
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293086C>T , CM000674.2:g.93293086C>T GRCh38
NC_000012.11:g.93686862C>T , CM000674.1:g.93686862C>T GRCh37
NC_000012.10:g.92210993C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34941G>A
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