Canonical Allele Identifier: CA2638676333
Gene:

Linked Data

gnomAD v4: 17-50211877-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211877C>A , CM000679.2:g.50211877C>A GRCh38
NC_000017.10:g.48289238C>A , CM000679.1:g.48289238C>A GRCh37
NC_000017.9:g.45644237C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1958C>A
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