Canonical Allele Identifier: CA8902497
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs145345722
ExAC: 18:13885140 C / A
gnomAD v2: 18-13885140-C-A
gnomAD v3: 18-13885141-C-A
gnomAD v4: 18-13885141-C-A
MyVariant Identifiers: chr18:g.13885140C>A (hg19) chr18:g.13885141C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885141C>A , CM000680.2:g.13885141C>A GRCh38
NC_000018.9:g.13885140C>A , CM000680.1:g.13885140C>A GRCh37
NC_000018.8:g.13875140C>A NCBI36
NG_011819.1:g.35396G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.378G>T MANE Select ENSP00000333821.2:p.Ala126=
ENST00000327606.3:c.378G>T ENSP00000333821.2:p.Ala126=
NM_000529.2:c.378G>T MANE Select NP_000520.1:p.Ala126=
NM_001291911.1:c.378G>T NP_001278840.1:p.Ala126=
XM_017025781.1:c.378G>T XP_016881270.1:p.Ala126=
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