Canonical Allele Identifier: CA2714008387
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471002

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198197A>T , CM000669.2:g.27198197A>T GRCh38
NC_000007.13:g.27237816A>T , CM000669.1:g.27237816A>T GRCh37
NC_000007.12:g.27204341A>T NCBI36
NG_008181.1:g.6910T>A
NG_008181.2:g.6910T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*1T>A MANE Select ENSP00000497112.1:n.*1T>A
ENST00000222753.5:c.*1T>A ENSP00000222753.4:n.*1T>A
NM_000522.4:c.*1T>A NP_000513.2:n.*1T>A
XM_011515344.1:c.*1T>A XP_011513646.1:n.*1T>A
NM_000522.5:c.*1T>A MANE Select NP_000513.2:n.*1T>A