Canonical Allele Identifier: CA406006740

Gene: TMEM91

Linked Data

• MyVariant Identifiers: chr19:g.41860115A>G (hg19) ; chr19:g.41354210A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354210A>G , CM000681.2:g.41354210A>G	GRCh38
NC_000019.9:g.41860115A>G , CM000681.1:g.41860115A>G	GRCh37
NC_000019.8:g.46551955A>G	NCBI36
NG_013091.1:g.14964T>C
NG_013364.1:g.4717T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3008A>G	ENSP00000441900.1:n.-30+3008A>G
ENST00000604123.5:c.37A>G	ENSP00000474871.1:p.Arg13Gly
ENST00000604424.1:n.350+3008A>G