Canonical Allele Identifier: CA358952743
Gene: MTNR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187455410G>C (hg19) chr4:g.186534256G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186534256G>C , CM000666.2:g.186534256G>C GRCh38
NC_000004.11:g.187455410G>C , CM000666.1:g.187455410G>C GRCh37
NC_000004.10:g.187692404G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703170.1:c.486C>G ENSP00000515216.1:p.Asn162Lys
ENST00000307161.5:c.486C>G MANE Select ENSP00000302811.5:p.Asn162Lys
ENST00000509111.2:c.147+20926C>G
NM_005958.3:c.486C>G NP_005949.1:p.Asn162Lys
XM_011532002.1:c.231C>G XP_011530304.1:p.Asn77Lys
XR_939589.1:n.1982-11388G>C
XR_939590.1:n.162-11388G>C
NM_005958.4:c.486C>G MANE Select NP_005949.1:p.Asn162Lys
XM_011532002.3:c.231C>G XP_011530304.1:p.Asn77Lys
XR_939589.2:n.1982-11388G>C
XR_939590.2:n.162-11388G>C
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