Canonical Allele Identifier: CA1573789060
Gene: MCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387951T= , CM000667.2:g.113387951T= GRCh38
NC_000005.9:g.112723648T= , CM000667.1:g.112723648T= GRCh37
NC_000005.8:g.112751547T= NCBI36
NG_012265.1:g.105880A=

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2739A= MANE Select ENSP00000386227.3:n.171-2739A=
ENST00000408903.6:c.171-2739A= ENSP00000386227.3:n.171-2739A=
NM_001085377.1:c.171-2739A= NP_001078846.1:n.171-2739A=
XM_017009473.1:c.171-2739A= XP_016864962.1:n.171-2739A=
NM_001085377.2:c.171-2739A= MANE Select NP_001078846.2:n.171-2739A=