Canonical Allele Identifier: CA1062643728
Gene:

Linked Data

dbSNP Id: rs553758400
gnomAD v3: 4-54228406-G-C
gnomAD v4: 4-54228406-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228406G>C , CM000666.2:g.54228406G>C GRCh38
NC_000004.11:g.55094573G>C , CM000666.1:g.55094573G>C GRCh37
NC_000004.10:g.54789330G>C NCBI36
NG_009250.1:g.4310G>C , LRG_309:g.4310G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46519G>C ENSP00000423325.1:n.1018-46519G>C