Canonical Allele Identifier: CA125026771
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs751176829
MyVariant Identifiers: chr5:g.113387955C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387955C>G , CM000667.2:g.113387955C>G GRCh38
NC_000005.9:g.112723652C>G , CM000667.1:g.112723652C>G GRCh37
NC_000005.8:g.112751551C>G NCBI36
NG_012265.1:g.105876G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2743G>C MANE Select ENSP00000386227.3:n.171-2743G>C
ENST00000408903.6:c.171-2743G>C ENSP00000386227.3:n.171-2743G>C
NM_001085377.1:c.171-2743G>C NP_001078846.1:n.171-2743G>C
XM_017009473.1:c.171-2743G>C XP_016864962.1:n.171-2743G>C
NM_001085377.2:c.171-2743G>C MANE Select NP_001078846.2:n.171-2743G>C
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