Canonical Allele Identifier: CA16238552
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1318772

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387870A>G , CM000667.2:g.113387870A>G GRCh38
NC_000005.9:g.112723567A>G , CM000667.1:g.112723567A>G GRCh37
NC_000005.8:g.112751466A>G NCBI36
NG_012265.1:g.105961T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2658T>C MANE Select ENSP00000386227.3:n.171-2658T>C
ENST00000408903.6:c.171-2658T>C ENSP00000386227.3:n.171-2658T>C
NM_001085377.1:c.171-2658T>C NP_001078846.1:n.171-2658T>C
XM_017009473.1:c.171-2658T>C XP_016864962.1:n.171-2658T>C
NM_001085377.2:c.171-2658T>C MANE Select NP_001078846.2:n.171-2658T>C