Canonical Allele Identifier: CA2737600921
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs2077844508

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46001412C>G , CM000683.2:g.46001412C>G GRCh38
NC_000021.8:g.47421326C>G , CM000683.1:g.47421326C>G GRCh37
NC_000021.7:g.46245754C>G NCBI36
NG_008674.1:g.24664C>G , LRG_475:g.24664C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463060.6:n.355+26C>G
ENST00000612273.2:c.82+26C>G
ENST00000682634.1:c.82+26C>G
ENST00000361866.8:c.1956+26C>G MANE Select ENSP00000355180.3:n.1956+26C>G
ENST00000361866.7:c.1956+26C>G ENSP00000355180.3:n.1956+26C>G
ENST00000463060.5:n.355+26C>G
ENST00000498614.5:n.190+26C>G
ENST00000612273.1:c.1950+26C>G ENSP00000483630.1:n.1950+26C>G
NM_001848.2:c.1956+26C>G , LRG_475t1:c.1956+26C>G NP_001839.2:n.1956+26C>G
NM_001848.3:c.1956+26C>G MANE Select NP_001839.2:n.1956+26C>G