Canonical Allele Identifier: CA566583916
Gene: GLP1R HGNC NCBI

Linked Data

dbSNP Id: rs1035321675
gnomAD v2: 6-39016578-C-T
gnomAD v4: 6-39048802-C-T
MyVariant Identifiers: chr6:g.39016578C>T (hg19) chr6:g.39048802C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39048802C>T , CM000668.2:g.39048802C>T GRCh38
NC_000006.11:g.39016578C>T , CM000668.1:g.39016578C>T GRCh37
NC_000006.10:g.39124556C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373256.5:c.-39C>T MANE Select ENSP00000362353.4:n.-39C>T
ENST00000373256.4:c.-39C>T ENSP00000362353.4:n.-39C>T
NM_002062.3:c.-39C>T NP_002053.3:n.-39C>T
XR_926153.1:n.22C>T
XR_926154.1:n.22C>T
XR_926155.1:n.22C>T
NM_002062.4:c.-39C>T NP_002053.3:n.-39C>T
NR_136562.1:n.22C>T
NR_136563.1:n.22C>T
NM_002062.5:c.-39C>T MANE Select NP_002053.3:n.-39C>T
NR_136562.2:n.22C>T
NR_136563.2:n.22C>T
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