Canonical Allele Identifier: CA30368480
Gene: TBX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.118961220C>A , CM000663.2:g.118961220C>A GRCh38
NC_000001.10:g.119503843C>A , CM000663.1:g.119503843C>A GRCh37
NC_000001.9:g.119305366C>A NCBI36
NG_013361.1:g.33337G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369429.5:c.205+26371G>T MANE Select ENSP00000358437.3:n.205+26371G>T
ENST00000207157.7:c.-114+28135G>T ENSP00000207157.3:n.-114+28135G>T
ENST00000369429.3:c.205+26371G>T ENSP00000358437.3:n.205+26371G>T
NM_152380.2:c.-114+28135G>T NP_689593.2:n.-114+28135G>T
XM_005271161.2:c.205+26371G>T XP_005271218.1:n.205+26371G>T
XM_005271162.1:c.205+26371G>T XP_005271219.1:n.205+26371G>T
NM_001330677.1:c.205+26371G>T NP_001317606.1:n.205+26371G>T
XM_005271161.4:c.205+26371G>T XP_005271218.1:n.205+26371G>T
NM_001330677.2:c.205+26371G>T MANE Select NP_001317606.1:n.205+26371G>T
NM_152380.3:c.-114+28135G>T NP_689593.2:n.-114+28135G>T