Canonical Allele Identifier: CA308527512

Gene: B9D2 TMEM91

Linked Data

• dbSNP Id: rs940196971
• gnomAD v4: 19-41363988-A-C
• MyVariant Identifiers: chr19:g.41869893A>C (hg19) ; chr19:g.41363988A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363988A>C , CM000681.2:g.41363988A>C	GRCh38
NC_000019.9:g.41869893A>C , CM000681.1:g.41869893A>C	GRCh37
NC_000019.8:g.46561733A>C	NCBI36
NG_013091.1:g.5186T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-35T>G (B9D2) MANE Select	ENSP00000243578.2:n.-35T>G
ENST00000243578.7:c.-35T>G (B9D2)	ENSP00000243578.2:n.-35T>G
ENST00000539627.5:c.-30+12786A>C (TMEM91)	ENSP00000441900.1:n.-30+12786A>C
ENST00000594416.1:c.-35T>G (B9D2)	ENSP00000469666.1:n.-35T>G
ENST00000601597.1:n.105T>G (B9D2)
ENST00000604123.5:c.142+9673A>C (TMEM91)	ENSP00000474871.1:n.142+9673A>C
ENST00000604424.1:n.350+12786A>C
NM_001098825.1:c.-137A>C (TMEM91)	NP_001092295.1:n.-137A>C
NM_030578.3:c.-35T>G (B9D2)	NP_085055.2:n.-35T>G
XM_006723405.1:c.-35T>G (B9D2)	XP_006723468.1:n.-35T>G
XM_011527350.1:c.-102T>G (B9D2)	XP_011525652.1:n.-102T>G
XM_011527350.2:c.-102T>G (B9D2)	XP_011525652.1:n.-102T>G
NM_030578.4:c.-35T>G (B9D2) MANE Select	NP_085055.2:n.-35T>G
NM_001369864.1:c.-394A>C (TMEM91)	NP_001356793.1:n.-394A>C
NM_001098825.2:c.-137A>C (TMEM91)	NP_001092295.1:n.-137A>C