Canonical Allele Identifier: CA1320446175
Gene:

Linked Data

dbSNP Id: rs2077889161
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033231G>A , CM000664.2:g.200033231G>A GRCh38
NC_000002.11:g.200897954G>A , CM000664.1:g.200897954G>A GRCh37
NC_000002.10:g.200606199G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22335C>T
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Search 100 bp 3'