Canonical Allele Identifier: CA11236171

Linked Data

dbSNP Id: rs13418078

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176151087C>T , CM000664.2:g.176151087C>T GRCh38
NC_000002.11:g.177015815C>T , CM000664.1:g.177015815C>T GRCh37
NC_000002.10:g.176724061C>T NCBI36
NG_012080.1:g.4703C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432796.2:c.-85+14088C>T (HOXD3) ENSP00000392615.2:n.-85+14088C>T
ENST00000468418.4:c.-547C>T ENSP00000424734.3:n.-547C>T
XM_005246510.3:c.-180-12986C>T (HOXD3) XP_005246567.1:n.-180-12986C>T
XM_005246514.3:c.-547C>T (HOXD4) XP_005246571.1:n.-547C>T
XM_006712477.2:c.-85+14088C>T (HOXD3) XP_006712540.1:n.-85+14088C>T
XM_005246514.4:c.-547C>T (HOXD4) XP_005246571.1:n.-547C>T