Canonical Allele Identifier: CA1573788970
Gene: MCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387831T= , CM000667.2:g.113387831T= GRCh38
NC_000005.9:g.112723528T= , CM000667.1:g.112723528T= GRCh37
NC_000005.8:g.112751427T= NCBI36
NG_012265.1:g.106000A=

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2619A= MANE Select ENSP00000386227.3:n.171-2619A=
ENST00000408903.6:c.171-2619A= ENSP00000386227.3:n.171-2619A=
NM_001085377.1:c.171-2619A= NP_001078846.1:n.171-2619A=
XM_017009473.1:c.171-2619A= XP_016864962.1:n.171-2619A=
NM_001085377.2:c.171-2619A= MANE Select NP_001078846.2:n.171-2619A=