Canonical Allele Identifier: CA406006968
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354298G>T , CM000681.2:g.41354298G>T GRCh38
NC_000019.9:g.41860203G>T , CM000681.1:g.41860203G>T GRCh37
NC_000019.8:g.46552043G>T NCBI36
NG_013091.1:g.14876C>A
NG_013364.1:g.4629C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3096G>T ENSP00000441900.1:n.-30+3096G>T
ENST00000604123.5:c.125G>T ENSP00000474871.1:p.Ser42Ile
ENST00000604424.1:n.350+3096G>T