Canonical Allele Identifier: CA401995172
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13885037T>A (hg19) chr18:g.13885038T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885038T>A , CM000680.2:g.13885038T>A GRCh38
NC_000018.9:g.13885037T>A , CM000680.1:g.13885037T>A GRCh37
NC_000018.8:g.13875037T>A NCBI36
NG_011819.1:g.35499A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.481A>T MANE Select ENSP00000333821.2:p.Thr161Ser
ENST00000327606.3:c.481A>T ENSP00000333821.2:p.Thr161Ser
NM_000529.2:c.481A>T MANE Select NP_000520.1:p.Thr161Ser
NM_001291911.1:c.481A>T NP_001278840.1:p.Thr161Ser
XM_017025781.1:c.481A>T XP_016881270.1:p.Thr161Ser
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