Canonical Allele Identifier: CA1573789010
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1769307627
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387877A>T , CM000667.2:g.113387877A>T GRCh38
NC_000005.9:g.112723574A>T , CM000667.1:g.112723574A>T GRCh37
NC_000005.8:g.112751473A>T NCBI36
NG_012265.1:g.105954T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2665T>A MANE Select ENSP00000386227.3:n.171-2665T>A
ENST00000408903.6:c.171-2665T>A ENSP00000386227.3:n.171-2665T>A
NM_001085377.1:c.171-2665T>A NP_001078846.1:n.171-2665T>A
XM_017009473.1:c.171-2665T>A XP_016864962.1:n.171-2665T>A
NM_001085377.2:c.171-2665T>A MANE Select NP_001078846.2:n.171-2665T>A
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