Canonical Allele Identifier: CA308527569

Gene: B9D2 TMEM91

Linked Data

• dbSNP Id: rs932368763
• gnomAD v4: 19-41364041-G-T
• MyVariant Identifiers: chr19:g.41364041G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41364041G>T , CM000681.2:g.41364041G>T	GRCh38
NC_000019.9:g.41869946G>T , CM000681.1:g.41869946G>T	GRCh37
NC_000019.8:g.46561786G>T	NCBI36
NG_013091.1:g.5133C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-88C>A (B9D2) MANE Select	ENSP00000243578.2:n.-88C>A
ENST00000243578.7:c.-88C>A (B9D2)	ENSP00000243578.2:n.-88C>A
ENST00000539627.5:c.-30+12839G>T (TMEM91)	ENSP00000441900.1:n.-30+12839G>T
ENST00000594416.1:c.-88C>A (B9D2)	ENSP00000469666.1:n.-88C>A
ENST00000601597.1:n.52C>A (B9D2)
ENST00000604123.5:c.142+9726G>T (TMEM91)	ENSP00000474871.1:n.142+9726G>T
ENST00000604424.1:n.350+12839G>T
NM_001098825.1:c.-84G>T (TMEM91)	NP_001092295.1:n.-84G>T
NM_030578.3:c.-88C>A (B9D2)	NP_085055.2:n.-88C>A
XM_006723405.1:c.-88C>A (B9D2)	XP_006723468.1:n.-88C>A
XM_011527350.1:c.-155C>A (B9D2)	XP_011525652.1:n.-155C>A
XM_011527350.2:c.-155C>A (B9D2)	XP_011525652.1:n.-155C>A
NM_030578.4:c.-88C>A (B9D2) MANE Select	NP_085055.2:n.-88C>A
NM_001369864.1:c.-341G>T (TMEM91)	NP_001356793.1:n.-341G>T
NM_001098825.2:c.-84G>T (TMEM91)	NP_001092295.1:n.-84G>T