Canonical Allele Identifier: CA406007001

Gene: TMEM91

Linked Data

• dbSNP Id: rs2038267848
• MyVariant Identifiers: chr19:g.41860217C>G (hg19) ; chr19:g.41354312C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354312C>G , CM000681.2:g.41354312C>G	GRCh38
NC_000019.9:g.41860217C>G , CM000681.1:g.41860217C>G	GRCh37
NC_000019.8:g.46552057C>G	NCBI36
NG_013091.1:g.14862G>C
NG_013364.1:g.4615G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3110C>G	ENSP00000441900.1:n.-30+3110C>G
ENST00000604123.5:c.139C>G	ENSP00000474871.1:p.Gln47Glu
ENST00000604424.1:n.350+3110C>G