Canonical Allele Identifier: CA2002397710
Gene:

Linked Data

dbSNP Id: rs1314959239
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072469C>T , CM000673.2:g.116072469C>T GRCh38
NC_000011.9:g.115943187C>T , CM000673.1:g.115943187C>T GRCh37
NC_000011.8:g.115448397C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+545G>A
XR_948056.1:n.311-5264G>A
XR_948057.1:n.97+640G>A
XR_001748401.1:n.192+545G>A
XR_948055.2:n.192+545G>A
XR_948056.2:n.314-5264G>A
XR_948057.2:n.97+640G>A
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