Canonical Allele Identifier: CA4198532
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs758828890
ExAC: 7:27237778 C / T
gnomAD v2: 7-27237778-C-T
MyVariant Identifiers: chr7:g.27237778C>T (hg19) chr7:g.27198159C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198159C>T , CM000669.2:g.27198159C>T GRCh38
NC_000007.13:g.27237778C>T , CM000669.1:g.27237778C>T GRCh37
NC_000007.12:g.27204303C>T NCBI36
NG_008181.1:g.6948G>A
NG_008181.2:g.6948G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*39G>A MANE Select ENSP00000497112.1:n.*39G>A
ENST00000222753.5:c.*39G>A ENSP00000222753.4:n.*39G>A
NM_000522.4:c.*39G>A NP_000513.2:n.*39G>A
XM_011515344.1:c.*39G>A XP_011513646.1:n.*39G>A
NM_000522.5:c.*39G>A MANE Select NP_000513.2:n.*39G>A
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