Canonical Allele Identifier: CA802100061

Gene: MCC

Linked Data

• dbSNP Id: rs1213338901
• MyVariant Identifiers: chr5:g.112723669C>G (hg19) ; chr5:g.113387972C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113387972C>G , CM000667.2:g.113387972C>G	GRCh38
NC_000005.9:g.112723669C>G , CM000667.1:g.112723669C>G	GRCh37
NC_000005.8:g.112751568C>G	NCBI36
NG_012265.1:g.105859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408903.7:c.171-2760G>C MANE Select	ENSP00000386227.3:n.171-2760G>C
ENST00000408903.6:c.171-2760G>C	ENSP00000386227.3:n.171-2760G>C
NM_001085377.1:c.171-2760G>C	NP_001078846.1:n.171-2760G>C
XM_017009473.1:c.171-2760G>C	XP_016864962.1:n.171-2760G>C
NM_001085377.2:c.171-2760G>C MANE Select	NP_001078846.2:n.171-2760G>C