Canonical Allele Identifier: CA1573789020
Gene: MCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387899C= , CM000667.2:g.113387899C= GRCh38
NC_000005.9:g.112723596C= , CM000667.1:g.112723596C= GRCh37
NC_000005.8:g.112751495C= NCBI36
NG_012265.1:g.105932G=

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2687G= MANE Select ENSP00000386227.3:n.171-2687G=
ENST00000408903.6:c.171-2687G= ENSP00000386227.3:n.171-2687G=
NM_001085377.1:c.171-2687G= NP_001078846.1:n.171-2687G=
XM_017009473.1:c.171-2687G= XP_016864962.1:n.171-2687G=
NM_001085377.2:c.171-2687G= MANE Select NP_001078846.2:n.171-2687G=