Canonical Allele Identifier: CA54648388
Gene:

Linked Data

dbSNP Id: rs199624562
MyVariant Identifiers: chr2:g.120332295G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332295G>A , CM000664.2:g.120332295G>A GRCh38
NC_000002.11:g.121089871G>A , CM000664.1:g.121089871G>A GRCh37
NC_000002.10:g.120806341G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3489G>A XP_011510609.1:n.141+3489G>A
Search 100 bp 5'
Search 100 bp 3'