Canonical Allele Identifier: CA406006714
Gene: TMEM91 HGNC NCBI

Linked Data

gnomAD v4: 19-41354204-C-A
MyVariant Identifiers: chr19:g.41860109C>A (hg19) chr19:g.41354204C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354204C>A , CM000681.2:g.41354204C>A GRCh38
NC_000019.9:g.41860109C>A , CM000681.1:g.41860109C>A GRCh37
NC_000019.8:g.46551949C>A NCBI36
NG_013091.1:g.14970G>T
NG_013364.1:g.4723G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3002C>A ENSP00000441900.1:n.-30+3002C>A
ENST00000604123.5:c.31C>A ENSP00000474871.1:p.His11Asn
ENST00000604424.1:n.350+3002C>A
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