Canonical Allele Identifier: CA1062643769
Gene:

Linked Data

dbSNP Id: rs1720486134
gnomAD v3: 4-54228520-T-C
gnomAD v4: 4-54228520-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228520T>C , CM000666.2:g.54228520T>C GRCh38
NC_000004.11:g.55094687T>C , CM000666.1:g.55094687T>C GRCh37
NC_000004.10:g.54789444T>C NCBI36
NG_009250.1:g.4424T>C , LRG_309:g.4424T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46405T>C ENSP00000423325.1:n.1018-46405T>C