Canonical Allele Identifier: CA2735810354
Gene:

Linked Data

dbSNP Id: rs2145370181
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522096T>A , CM000681.2:g.33522096T>A GRCh38
NC_000019.9:g.34013002T>A , CM000681.1:g.34013002T>A GRCh37
NC_000019.8:g.38704842T>A NCBI36
NG_013358.1:g.4798A>T
NG_013358.2:g.4798A>T

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.73+82T>A
XR_935919.1:n.72+78T>A
XR_001754035.2:n.81+82T>A
XR_935918.2:n.81+82T>A
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