Canonical Allele Identifier: CA2638676337
Gene:

Linked Data

gnomAD v4: 17-50211881-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211881C>A , CM000679.2:g.50211881C>A GRCh38
NC_000017.10:g.48289242C>A , CM000679.1:g.48289242C>A GRCh37
NC_000017.9:g.45644241C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1954C>A
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