Canonical Allele Identifier: CA507559449
Gene: TMEM91 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41860111C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354206C>T , CM000681.2:g.41354206C>T GRCh38
NC_000019.9:g.41860111C>T , CM000681.1:g.41860111C>T GRCh37
NC_000019.8:g.46551951C>T NCBI36
NG_013091.1:g.14968G>A
NG_013364.1:g.4721G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3004C>T ENSP00000441900.1:n.-30+3004C>T
ENST00000604123.5:c.33C>T ENSP00000474871.1:p.His11=
ENST00000604424.1:n.350+3004C>T