Canonical Allele Identifier: CA507559773
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs2038267366
MyVariant Identifiers: chr19:g.41860198G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354293G>A , CM000681.2:g.41354293G>A GRCh38
NC_000019.9:g.41860198G>A , CM000681.1:g.41860198G>A GRCh37
NC_000019.8:g.46552038G>A NCBI36
NG_013091.1:g.14881C>T
NG_013364.1:g.4634C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3091G>A ENSP00000441900.1:n.-30+3091G>A
ENST00000604123.5:c.120G>A ENSP00000474871.1:p.Lys40=
ENST00000604424.1:n.350+3091G>A