Canonical Allele Identifier: CA802100085
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1419352934
gnomAD v3: 5-113388040-G-A
gnomAD v4: 5-113388040-G-A
MyVariant Identifiers: chr5:g.112723737G>A (hg19) chr5:g.113388040G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113388040G>A , CM000667.2:g.113388040G>A GRCh38
NC_000005.9:g.112723737G>A , CM000667.1:g.112723737G>A GRCh37
NC_000005.8:g.112751636G>A NCBI36
NG_012265.1:g.105791C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2828C>T MANE Select ENSP00000386227.3:n.171-2828C>T
ENST00000408903.6:c.171-2828C>T ENSP00000386227.3:n.171-2828C>T
NM_001085377.1:c.171-2828C>T NP_001078846.1:n.171-2828C>T
XM_017009473.1:c.171-2828C>T XP_016864962.1:n.171-2828C>T
NM_001085377.2:c.171-2828C>T MANE Select NP_001078846.2:n.171-2828C>T
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