Canonical Allele Identifier: CA358952746
Gene: MTNR1A HGNC NCBI

Linked Data

dbSNP Id: rs1199505841
gnomAD v2: 4-187455411-T-C
gnomAD v3: 4-186534257-T-C
gnomAD v4: 4-186534257-T-C
MyVariant Identifiers: chr4:g.187455411T>C (hg19) chr4:g.186534257T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186534257T>C , CM000666.2:g.186534257T>C GRCh38
NC_000004.11:g.187455411T>C , CM000666.1:g.187455411T>C GRCh37
NC_000004.10:g.187692405T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703170.1:c.485A>G ENSP00000515216.1:p.Asn162Ser
ENST00000307161.5:c.485A>G MANE Select ENSP00000302811.5:p.Asn162Ser
ENST00000509111.2:c.147+20925A>G
NM_005958.3:c.485A>G NP_005949.1:p.Asn162Ser
XM_011532002.1:c.230A>G XP_011530304.1:p.Asn77Ser
XR_939589.1:n.1982-11387T>C
XR_939590.1:n.162-11387T>C
NM_005958.4:c.485A>G MANE Select NP_005949.1:p.Asn162Ser
XM_011532002.3:c.230A>G XP_011530304.1:p.Asn77Ser
XR_939589.2:n.1982-11387T>C
XR_939590.2:n.162-11387T>C
Search 100 bp 5'
Search 100 bp 3'