Canonical Allele Identifier: CA97374085
Gene:

Linked Data

dbSNP Id: rs1014456662
gnomAD v3: 4-54072297-A-G
gnomAD v4: 4-54072297-A-G
MyVariant Identifiers: chr4:g.54072297A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072297A>G , CM000666.2:g.54072297A>G GRCh38
NC_000004.11:g.54938464A>G , CM000666.1:g.54938464A>G GRCh37
NC_000004.10:g.54633221A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202628A>G ENSP00000423325.1:n.1018-202628A>G