Canonical Allele Identifier: CA1573789056
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1769308904

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387948dup , CM000667.2:g.113387948dup GRCh38
NC_000005.9:g.112723645dup , CM000667.1:g.112723645dup GRCh37
NC_000005.8:g.112751544dup NCBI36
NG_012265.1:g.105883dup

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2736dup MANE Select ENSP00000386227.3:n.171-2736dup
ENST00000408903.6:c.171-2736dup ENSP00000386227.3:n.171-2736dup
NM_001085377.1:c.171-2736dup NP_001078846.1:n.171-2736dup
XM_017009473.1:c.171-2736dup XP_016864962.1:n.171-2736dup
NM_001085377.2:c.171-2736dup MANE Select NP_001078846.2:n.171-2736dup