Canonical Allele Identifier: CA401995106
Gene: MC2R HGNC NCBI

Linked Data

gnomAD v4: 18-13885008-G-A
MyVariant Identifiers: chr18:g.13885007G>A (hg19) chr18:g.13885008G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885008G>A , CM000680.2:g.13885008G>A GRCh38
NC_000018.9:g.13885007G>A , CM000680.1:g.13885007G>A GRCh37
NC_000018.8:g.13875007G>A NCBI36
NG_011819.1:g.35529C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.511C>T MANE Select ENSP00000333821.2:p.His171Tyr
ENST00000327606.3:c.511C>T ENSP00000333821.2:p.His171Tyr
NM_000529.2:c.511C>T MANE Select NP_000520.1:p.His171Tyr
NM_001291911.1:c.511C>T NP_001278840.1:p.His171Tyr
XM_017025781.1:c.511C>T XP_016881270.1:p.His171Tyr
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