Canonical Allele Identifier: CA2739311025
Gene: MTNR1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.92972141C>A , CM000673.2:g.92972141C>A GRCh38
NC_000011.9:g.92705307C>A , CM000673.1:g.92705307C>A GRCh37
NC_000011.8:g.92344955C>A NCBI36
NG_028160.1:g.7519C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257068.3:c.223+2193C>A MANE Select ENSP00000257068.2:n.223+2193C>A
ENST00000257068.2:c.223+2193C>A ENSP00000257068.2:n.223+2193C>A
ENST00000528076.1:c.165+2193C>A
ENST00000532482.1:c.224-320C>A ENSP00000436101.1:n.224-320C>A
NM_005959.3:c.223+2193C>A NP_005950.1:n.223+2193C>A
XM_011542839.1:c.223+2193C>A XP_011541141.1:n.223+2193C>A
XM_011542839.2:c.223+2193C>A XP_011541141.1:n.223+2193C>A
NM_005959.5:c.223+2193C>A MANE Select NP_005950.1:n.223+2193C>A
Search 100 bp 5'
Search 100 bp 3'