Canonical Allele Identifier: CA289293213
Gene:

Linked Data

dbSNP Id: rs895998414
MyVariant Identifiers: chr17:g.28564079G>A (hg19) chr17:g.30237061G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237061G>A , CM000679.2:g.30237061G>A GRCh38
NC_000017.10:g.28564079G>A , CM000679.1:g.28564079G>A GRCh37
NC_000017.9:g.25588205G>A NCBI36
NG_011747.2:g.3876C>T

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.156G>A
XR_001752824.1:n.271G>A
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