Canonical Allele Identifier: CA406007006
Gene: TMEM91 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41860219A>C (hg19) chr19:g.41354314A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354314A>C , CM000681.2:g.41354314A>C GRCh38
NC_000019.9:g.41860219A>C , CM000681.1:g.41860219A>C GRCh37
NC_000019.8:g.46552059A>C NCBI36
NG_013091.1:g.14860T>G
NG_013364.1:g.4613T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3112A>C ENSP00000441900.1:n.-30+3112A>C
ENST00000604123.5:c.141A>C ENSP00000474871.1:p.Gln47His
ENST00000604424.1:n.350+3112A>C
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