Canonical Allele Identifier: CA406006969
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs1465090720
gnomAD v4: 19-41354299-T-A
MyVariant Identifiers: chr19:g.41860204T>A (hg19) chr19:g.41354299T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354299T>A , CM000681.2:g.41354299T>A GRCh38
NC_000019.9:g.41860204T>A , CM000681.1:g.41860204T>A GRCh37
NC_000019.8:g.46552044T>A NCBI36
NG_013091.1:g.14875A>T
NG_013364.1:g.4628A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3097T>A ENSP00000441900.1:n.-30+3097T>A
ENST00000604123.5:c.126T>A ENSP00000474871.1:p.Ser42Arg
ENST00000604424.1:n.350+3097T>A
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