Canonical Allele Identifier: CA1048013698
Gene:

Linked Data

gnomAD v3: 3-53057056-C-G
gnomAD v4: 3-53057056-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057056C>G , CM000665.2:g.53057056C>G GRCh38
NC_000003.11:g.53091072C>G , CM000665.1:g.53091072C>G GRCh37
NC_000003.10:g.53066112C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9817G>C
ENST00000607283.5:c.465-13802G>C
ENST00000607495.5:c.447+20632G>C