Canonical Allele Identifier: CA216292207
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs902219463
gnomAD v3: 11-2444444-G-A
gnomAD v4: 11-2444444-G-A
MyVariant Identifiers: chr11:g.2465674G>A (hg19) chr11:g.2444444G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444444G>A , CM000673.2:g.2444444G>A GRCh38
NC_000011.9:g.2465674G>A , CM000673.1:g.2465674G>A GRCh37
NC_000011.8:g.2422250G>A NCBI36
NG_008935.1:g.4454G>A , LRG_287:g.4454G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.-1699C>T MANE Select ENSP00000512529.1:n.-1699C>T
XR_930984.1:n.127C>T
NM_014555.4:c.-1699C>T MANE Select NP_055370.1:n.-1699C>T
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