Canonical Allele Identifier: CA1320446146
Gene:

Linked Data

dbSNP Id: rs2077888941
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033171C>T , CM000664.2:g.200033171C>T GRCh38
NC_000002.11:g.200897894C>T , CM000664.1:g.200897894C>T GRCh37
NC_000002.10:g.200606139C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22275G>A
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