Canonical Allele Identifier: CA2814189187
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521943G>T , CM000681.2:g.33521943G>T GRCh38
NC_000019.9:g.34012849G>T , CM000681.1:g.34012849G>T GRCh37
NC_000019.8:g.38704689G>T NCBI36
NG_013358.1:g.4951C>A
NG_013358.2:g.4951C>A

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.2G>T
XR_001754035.2:n.10G>T
XR_935918.2:n.10G>T
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