Canonical Allele Identifier: CA1696262956

Gene: HOXA13

Linked Data

• dbSNP Id: rs1784026222

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27198077T>C , CM000669.2:g.27198077T>C	GRCh38
NC_000007.13:g.27237696T>C , CM000669.1:g.27237696T>C	GRCh37
NC_000007.12:g.27204221T>C	NCBI36
NG_008181.1:g.7030A>G
NG_008181.2:g.7030A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649031.1:c.*121A>G MANE Select	ENSP00000497112.1:n.*121A>G
ENST00000222753.5:c.*121A>G	ENSP00000222753.4:n.*121A>G
NM_000522.4:c.*121A>G	NP_000513.2:n.*121A>G
XM_011515344.1:c.*121A>G	XP_011513646.1:n.*121A>G
NM_000522.5:c.*121A>G MANE Select	NP_000513.2:n.*121A>G