Canonical Allele Identifier: CA1041166023
Gene:

Linked Data

dbSNP Id: rs1559327398
gnomAD v3: 2-200033145-C-A
gnomAD v4: 2-200033145-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033145C>A , CM000664.2:g.200033145C>A GRCh38
NC_000002.11:g.200897868C>A , CM000664.1:g.200897868C>A GRCh37
NC_000002.10:g.200606113C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22249G>T
Search 100 bp 5'
Search 100 bp 3'