Canonical Allele Identifier: CA2714008370
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471001
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198196C>G , CM000669.2:g.27198196C>G GRCh38
NC_000007.13:g.27237815C>G , CM000669.1:g.27237815C>G GRCh37
NC_000007.12:g.27204340C>G NCBI36
NG_008181.1:g.6911G>C
NG_008181.2:g.6911G>C

Transcript Alleles

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