Canonical Allele Identifier: CA2682147606
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471001
gnomAD v4: 7-27198196-C-T
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Genomic Alleles

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

Transcript Alleles

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