Canonical Allele Identifier: CA54648382
Gene:

Linked Data

dbSNP Id: rs546567554
gnomAD v2: 2-121089858-G-A
gnomAD v3: 2-120332282-G-A
gnomAD v4: 2-120332282-G-A
MyVariant Identifiers: chr2:g.121089858G>A (hg19) chr2:g.120332282G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332282G>A , CM000664.2:g.120332282G>A GRCh38
NC_000002.11:g.121089858G>A , CM000664.1:g.121089858G>A GRCh37
NC_000002.10:g.120806328G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3476G>A XP_011510609.1:n.141+3476G>A
Search 100 bp 5'
Search 100 bp 3'