Canonical Allele Identifier: CA401994214
Gene: MC2R HGNC NCBI

Linked Data

gnomAD v4: 18-13884794-A-G
MyVariant Identifiers: chr18:g.13884793A>G (hg19) chr18:g.13884794A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884794A>G , CM000680.2:g.13884794A>G GRCh38
NC_000018.9:g.13884793A>G , CM000680.1:g.13884793A>G GRCh37
NC_000018.8:g.13874793A>G NCBI36
NG_011819.1:g.35743T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.725T>C MANE Select ENSP00000333821.2:p.Met242Thr
ENST00000327606.3:c.725T>C ENSP00000333821.2:p.Met242Thr
NM_000529.2:c.725T>C MANE Select NP_000520.1:p.Met242Thr
NM_001291911.1:c.725T>C NP_001278840.1:p.Met242Thr
XM_017025781.1:c.725T>C XP_016881270.1:p.Met242Thr
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