Canonical Allele Identifier: CA573409574
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1284324156
gnomAD v2: 7-27237791-T-C
gnomAD v4: 7-27198172-T-C
MyVariant Identifiers: chr7:g.27237791T>C (hg19) chr7:g.27198172T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198172T>C , CM000669.2:g.27198172T>C GRCh38
NC_000007.13:g.27237791T>C , CM000669.1:g.27237791T>C GRCh37
NC_000007.12:g.27204316T>C NCBI36
NG_008181.1:g.6935A>G
NG_008181.2:g.6935A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*26A>G MANE Select ENSP00000497112.1:n.*26A>G
ENST00000222753.5:c.*26A>G ENSP00000222753.4:n.*26A>G
NM_000522.4:c.*26A>G NP_000513.2:n.*26A>G
XM_011515344.1:c.*26A>G XP_011513646.1:n.*26A>G
NM_000522.5:c.*26A>G MANE Select NP_000513.2:n.*26A>G
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