Canonical Allele Identifier: CA216292211
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs900202781
gnomAD v3: 11-2444464-C-T
gnomAD v4: 11-2444464-C-T
MyVariant Identifiers: chr11:g.2465694C>T (hg19) chr11:g.2444464C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444464C>T , CM000673.2:g.2444464C>T GRCh38
NC_000011.9:g.2465694C>T , CM000673.1:g.2465694C>T GRCh37
NC_000011.8:g.2422270C>T NCBI36
NG_008935.1:g.4474C>T , LRG_287:g.4474C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.-1719G>A MANE Select ENSP00000512529.1:n.-1719G>A
XR_930984.1:n.107G>A
NM_014555.4:c.-1719G>A MANE Select NP_055370.1:n.-1719G>A
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