Canonical Allele Identifier: CA2336427040
Community Standard Title: NC_000019.10:g.41354391A=
Gene: TMEM91 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354391A= , CM000681.2:g.41354391A= GRCh38
NC_000019.9:g.41860296A= , CM000681.1:g.41860296A= GRCh37
NC_000019.8:g.46552136A= NCBI36
NG_013091.1:g.14783T=
NG_013364.1:g.4536T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3189A= ENSP00000441900.1:n.-30+3189A=
ENST00000604123.5:c.142+76A= ENSP00000474871.1:n.142+76A=
ENST00000604424.1:n.350+3189A=