Canonical Allele Identifier: CA14950946
Gene: HMGXB4 HGNC NCBI

Linked Data

dbSNP Id: rs2413338

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267530C>T , CM000684.2:g.35267530C>T GRCh38
NC_000022.10:g.35663523C>T , CM000684.1:g.35663523C>T GRCh37
NC_000022.9:g.33993523C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216106.6:c.1215+1927C>T MANE Select ENSP00000216106.5:n.1215+1927C>T
ENST00000216106.5:c.1215+1927C>T ENSP00000216106.5:n.1215+1927C>T
ENST00000418170.5:c.*1051+1927C>T ENSP00000395532.1:n.*1051+1927C>T
NM_001003681.2:c.1215+1927C>T NP_001003681.1:n.1215+1927C>T
NR_027780.1:n.1504+1927C>T
XM_006724100.2:c.1344+1927C>T XP_006724163.1:n.1344+1927C>T
XM_006724101.2:c.1344+1927C>T XP_006724164.1:n.1344+1927C>T
XM_006724102.1:c.888+1927C>T XP_006724165.1:n.888+1927C>T
XM_011529817.1:c.1215+1927C>T XP_011528119.1:n.1215+1927C>T
NM_001362972.1:c.888+1927C>T NP_001349901.1:n.888+1927C>T
XM_006724100.4:c.1344+1927C>T XP_006724163.1:n.1344+1927C>T
XM_006724101.4:c.1344+1927C>T XP_006724164.1:n.1344+1927C>T
XM_006724102.2:c.888+1927C>T XP_006724165.1:n.888+1927C>T
NM_001003681.3:c.1215+1927C>T MANE Select NP_001003681.1:n.1215+1927C>T
NM_001362972.2:c.888+1927C>T NP_001349901.1:n.888+1927C>T
NR_027780.2:n.1463+1927C>T