Canonical Allele Identifier: CA406006961
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354296G>T , CM000681.2:g.41354296G>T GRCh38
NC_000019.9:g.41860201G>T , CM000681.1:g.41860201G>T GRCh37
NC_000019.8:g.46552041G>T NCBI36
NG_013091.1:g.14878C>A
NG_013364.1:g.4631C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3094G>T ENSP00000441900.1:n.-30+3094G>T
ENST00000604123.5:c.123G>T ENSP00000474871.1:p.Glu41Asp
ENST00000604424.1:n.350+3094G>T