Canonical Allele Identifier: CA1107981949

Gene: TMEM178B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141188521C>T , CM000669.2:g.141188521C>T	GRCh38
NC_000007.13:g.140888321C>T , CM000669.1:g.140888321C>T	GRCh37
NC_000007.12:g.140534790C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565468.6:c.383-24070C>T MANE Select	ENSP00000456594.1:n.383-24070C>T
ENST00000563442.1:n.301-24070C>T
ENST00000565468.5:c.383-24070C>T	ENSP00000456594.1:n.383-24070C>T
ENST00000610315.1:c.383-24070C>T	ENSP00000484025.1:n.383-24070C>T
NM_001195278.1:c.383-24070C>T	NP_001182207.1:n.383-24070C>T
XM_011515705.1:c.383-24070C>T	XP_011514007.1:n.383-24070C>T
XR_927317.1:n.1383-24070C>T
XM_011515705.2:c.383-24070C>T	XP_011514007.1:n.383-24070C>T
XM_017011636.1:c.383-24070C>T	XP_016867125.1:n.383-24070C>T
XR_001744505.1:n.1286-24070C>T
NM_001195278.2:c.383-24070C>T MANE Select	NP_001182207.1:n.383-24070C>T