Canonical Allele Identifier: CA406006972
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354300C>G , CM000681.2:g.41354300C>G GRCh38
NC_000019.9:g.41860205C>G , CM000681.1:g.41860205C>G GRCh37
NC_000019.8:g.46552045C>G NCBI36
NG_013091.1:g.14874G>C
NG_013364.1:g.4627G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3098C>G ENSP00000441900.1:n.-30+3098C>G
ENST00000604123.5:c.127C>G ENSP00000474871.1:p.Gln43Glu
ENST00000604424.1:n.350+3098C>G