Canonical Allele Identifier: CA1233617215
Gene:

Linked Data

dbSNP Id: rs1681158018
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554170G>A , CM000664.2:g.1554170G>A GRCh38
NC_000002.11:g.1557942G>A , CM000664.1:g.1557942G>A GRCh37
NC_000002.10:g.1536949G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510447.1:c.-1003G>A XP_011508749.1:n.-1003G>A
XM_011510448.1:c.-1003G>A XP_011508750.1:n.-1003G>A
XR_922720.1:n.85+2328C>T
XM_017005455.1:c.-1003G>A XP_016860944.1:n.-1003G>A
NR_168373.1:n.746G>A
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