Canonical Allele Identifier: CA507559851

Gene: TMEM91

Linked Data

• gnomAD v4: 19-41354314-A-G
• MyVariant Identifiers: chr19:g.41860219A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354314A>G , CM000681.2:g.41354314A>G	GRCh38
NC_000019.9:g.41860219A>G , CM000681.1:g.41860219A>G	GRCh37
NC_000019.8:g.46552059A>G	NCBI36
NG_013091.1:g.14860T>C
NG_013364.1:g.4613T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3112A>G	ENSP00000441900.1:n.-30+3112A>G
ENST00000604123.5:c.141A>G	ENSP00000474871.1:p.Gln47=
ENST00000604424.1:n.350+3112A>G