Canonical Allele Identifier: CA836505564
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs1487952905
MyVariant Identifiers: chr7:g.20203829G>C (hg19) chr7:g.20164206G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164206G>C , CM000669.2:g.20164206G>C GRCh38
NC_000007.13:g.20203829G>C , CM000669.1:g.20203829G>C GRCh37
NC_000007.12:g.20170354G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9+50C>G MANE Select ENSP00000383185.3:n.-9+50C>G
ENST00000332878.8:c.-8-2336C>G ENSP00000328410.4:n.-8-2336C>G
ENST00000400331.9:c.-9+50C>G ENSP00000383185.3:n.-9+50C>G
ENST00000589011.1:c.-8-2336C>G ENSP00000466864.1:n.-8-2336C>G
NM_182762.3:c.-9+50C>G NP_877439.3:n.-9+50C>G
NM_182762.4:c.-9+50C>G MANE Select NP_877439.3:n.-9+50C>G
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