Canonical Allele Identifier: CA367069666
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1398380500
gnomAD v2: 7-27237881-A-G
gnomAD v4: 7-27198262-A-G
MyVariant Identifiers: chr7:g.27237881A>G (hg19) chr7:g.27198262A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198262A>G , CM000669.2:g.27198262A>G GRCh38
NC_000007.13:g.27237881A>G , CM000669.1:g.27237881A>G GRCh37
NC_000007.12:g.27204406A>G NCBI36
NG_008181.1:g.6845T>C
NG_008181.2:g.6845T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1103T>C MANE Select ENSP00000497112.1:p.Ile368Thr
ENST00000222753.5:c.1103T>C ENSP00000222753.4:p.Ile368Thr
NM_000522.4:c.1103T>C NP_000513.2:p.Ile368Thr
XM_011515344.1:c.1103T>C XP_011513646.1:p.Ile368Thr
NM_000522.5:c.1103T>C MANE Select NP_000513.2:p.Ile368Thr
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