Canonical Allele Identifier: CA8255723
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 470710
ClinVar RCV Id: RCV000552416
dbSNP Id: rs200051702
ExAC: 16:89986391 C / T
gnomAD v2: 16-89986391-C-T
gnomAD v3: 16-89919983-C-T
gnomAD v4: 16-89919983-C-T
MyVariant Identifiers: chr16:g.89986391C>T (hg19) chr16:g.89919983C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919983C>T , CM000678.2:g.89919983C>T GRCh38
NC_000016.9:g.89986391C>T , CM000678.1:g.89986391C>T GRCh37
NC_000016.8:g.88513892C>T NCBI36
NG_012026.1:g.7105C>T
NG_027810.1:g.2975C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.725C>T MANE Select ENSP00000451605.1:p.Thr242Ile
ENST00000639847.1:c.725C>T ENSP00000492011.1:p.Thr242Ile
ENST00000555147.1:c.725C>T ENSP00000451605.1:p.Thr242Ile
ENST00000555427.1:c.725C>T ENSP00000451760.1:p.Thr242Ile
ENST00000556922.1:c.725C>T ENSP00000451560.1:p.Thr242Ile
NM_002386.3:c.725C>T NP_002377.4:p.Thr242Ile
NM_002386.4:c.725C>T MANE Select NP_002377.4:p.Thr242Ile
Search 100 bp 5'
Search 100 bp 3'