Canonical Allele Identifier: CA397459235
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2175946
ClinVar RCV Id: RCV002605869
dbSNP Id: rs2045689907
gnomAD v4: 16-89919344-A-G
MyVariant Identifiers: chr16:g.89985752A>G (hg19) chr16:g.89919344A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919344A>G , CM000678.2:g.89919344A>G GRCh38
NC_000016.9:g.89985752A>G , CM000678.1:g.89985752A>G GRCh37
NC_000016.8:g.88513253A>G NCBI36
NG_012026.1:g.6466A>G
NG_027810.1:g.2336A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.86A>G MANE Select ENSP00000451605.1:p.Asn29Ser
ENST00000639847.1:c.86A>G ENSP00000492011.1:p.Asn29Ser
ENST00000555147.1:c.86A>G ENSP00000451605.1:p.Asn29Ser
ENST00000555427.1:c.86A>G ENSP00000451760.1:p.Asn29Ser
ENST00000556922.1:c.86A>G ENSP00000451560.1:p.Asn29Ser
NM_002386.3:c.86A>G NP_002377.4:p.Asn29Ser
NM_002386.4:c.86A>G MANE Select NP_002377.4:p.Asn29Ser
Search 100 bp 5'
Search 100 bp 3'