Canonical Allele Identifier: CA367075780
Gene: HOXA2 HGNC NCBI

Linked Data

dbSNP Id: rs119489104

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27101301G>A , CM000669.2:g.27101301G>A GRCh38
NC_000007.13:g.27140920G>A , CM000669.1:g.27140920G>A GRCh37
NC_000007.12:g.27107445G>A NCBI36
NG_012078.1:g.6475C>T
NG_033087.1:g.10208G>A
NG_012078.2:g.6475C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000222718.7:c.556C>T MANE Select ENSP00000222718.5:p.Gln186Ter
ENST00000222718.6:c.556C>T ENSP00000222718.5:p.Gln186Ter
ENST00000612779.1:n.1386C>T
NM_006735.3:c.556C>T NP_006726.1:p.Gln186Ter
NM_006735.4:c.556C>T MANE Select NP_006726.1:p.Gln186Ter