Canonical Allele Identifier: CA597098383
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs1171873528
gnomAD v2: 11-2465699-C-G
gnomAD v3: 11-2444469-C-G
gnomAD v4: 11-2444469-C-G
MyVariant Identifiers: chr11:g.2465699C>G (hg19) chr11:g.2444469C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444469C>G , CM000673.2:g.2444469C>G GRCh38
NC_000011.9:g.2465699C>G , CM000673.1:g.2465699C>G GRCh37
NC_000011.8:g.2422275C>G NCBI36
NG_008935.1:g.4479C>G , LRG_287:g.4479C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.-1724G>C MANE Select ENSP00000512529.1:n.-1724G>C
XR_930984.1:n.102G>C
NM_014555.4:c.-1724G>C MANE Select NP_055370.1:n.-1724G>C
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