Canonical Allele Identifier: CA1481405742
Gene:

Linked Data

dbSNP Id: rs1738884100
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499820G>T , CM000666.2:g.102499820G>T GRCh38
NC_000004.11:g.103420977G>T , CM000666.1:g.103420977G>T GRCh37
NC_000004.10:g.103640009G>T NCBI36
NG_050628.1:g.3492G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1429C>A XP_011530769.1:n.643+1429C>A
NR_136202.1:n.48+2619C>A
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