Canonical Allele Identifier: CA308519867
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs761713975
gnomAD v4: 19-41354202-G-A
MyVariant Identifiers: chr19:g.41860107G>A (hg19) chr19:g.41354202G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354202G>A , CM000681.2:g.41354202G>A GRCh38
NC_000019.9:g.41860107G>A , CM000681.1:g.41860107G>A GRCh37
NC_000019.8:g.46551947G>A NCBI36
NG_013091.1:g.14972C>T
NG_013364.1:g.4725C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3000G>A ENSP00000441900.1:n.-30+3000G>A
ENST00000604123.5:c.29G>A ENSP00000474871.1:p.Gly10Asp
ENST00000604424.1:n.350+3000G>A
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