Canonical Allele Identifier: CA308519934
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs531243977
gnomAD v2: 19-41860211-G-A
gnomAD v3: 19-41354306-G-A
gnomAD v4: 19-41354306-G-A
MyVariant Identifiers: chr19:g.41860211G>A (hg19) chr19:g.41354306G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354306G>A , CM000681.2:g.41354306G>A GRCh38
NC_000019.9:g.41860211G>A , CM000681.1:g.41860211G>A GRCh37
NC_000019.8:g.46552051G>A NCBI36
NG_013091.1:g.14868C>T
NG_013364.1:g.4621C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3104G>A ENSP00000441900.1:n.-30+3104G>A
ENST00000604123.5:c.133G>A ENSP00000474871.1:p.Gly45Arg
ENST00000604424.1:n.350+3104G>A
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