Canonical Allele Identifier: CA406006708
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs1457749814
gnomAD v2: 19-41860106-G-C
gnomAD v4: 19-41354201-G-C
MyVariant Identifiers: chr19:g.41860106G>C (hg19) chr19:g.41354201G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354201G>C , CM000681.2:g.41354201G>C GRCh38
NC_000019.9:g.41860106G>C , CM000681.1:g.41860106G>C GRCh37
NC_000019.8:g.46551946G>C NCBI36
NG_013091.1:g.14973C>G
NG_013364.1:g.4726C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+2999G>C ENSP00000441900.1:n.-30+2999G>C
ENST00000604123.5:c.28G>C ENSP00000474871.1:p.Gly10Arg
ENST00000604424.1:n.350+2999G>C
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