Canonical Allele Identifier: CA406006978
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354302G>C , CM000681.2:g.41354302G>C GRCh38
NC_000019.9:g.41860207G>C , CM000681.1:g.41860207G>C GRCh37
NC_000019.8:g.46552047G>C NCBI36
NG_013091.1:g.14872C>G
NG_013364.1:g.4625C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3100G>C ENSP00000441900.1:n.-30+3100G>C
ENST00000604123.5:c.129G>C ENSP00000474871.1:p.Gln43His
ENST00000604424.1:n.350+3100G>C