Canonical Allele Identifier: CA11488660
Gene: MCCC1 HGNC NCBI

Linked Data

dbSNP Id: rs11711441

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183103487G>A , CM000665.2:g.183103487G>A GRCh38
NC_000003.11:g.182821275G>A , CM000665.1:g.182821275G>A GRCh37
NC_000003.10:g.184303969G>A NCBI36
NG_008100.1:g.1091C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000492597.5:c.-101-8882C>T ENSP00000419898.1:n.-101-8882C>T