Canonical Allele Identifier: CA406006724

Gene: TMEM91

Linked Data

• MyVariant Identifiers: chr19:g.41860111C>A (hg19) ; chr19:g.41354206C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3004C>A	ENSP00000441900.1:n.-30+3004C>A
ENST00000604123.5:c.33C>A	ENSP00000474871.1:p.His11Gln
ENST00000604424.1:n.350+3004C>A