Canonical Allele Identifier: CA367069700

Gene: HOXA13

Linked Data

• dbSNP Id: rs2115471189
• MyVariant Identifiers: chr7:g.27237897C>A (hg19) ; chr7:g.27198278C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27198278C>A , CM000669.2:g.27198278C>A	GRCh38
NC_000007.13:g.27237897C>A , CM000669.1:g.27237897C>A	GRCh37
NC_000007.12:g.27204422C>A	NCBI36
NG_008181.1:g.6829G>T
NG_008181.2:g.6829G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649031.1:c.1087G>T MANE Select	ENSP00000497112.1:p.Glu363Ter
ENST00000222753.5:c.1087G>T	ENSP00000222753.4:p.Glu363Ter
NM_000522.4:c.1087G>T	NP_000513.2:p.Glu363Ter
XM_011515344.1:c.1087G>T	XP_011513646.1:p.Glu363Ter
NM_000522.5:c.1087G>T MANE Select	NP_000513.2:p.Glu363Ter