Canonical Allele Identifier: CA1468682088
Gene:

Linked Data

dbSNP Id: rs1721060485
gnomAD v3: 4-74554016-A-G
gnomAD v4: 4-74554016-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554016A>G , CM000666.2:g.74554016A>G GRCh38
NC_000004.11:g.75419733A>G , CM000666.1:g.75419733A>G GRCh37
NC_000004.10:g.75638597A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1184T>C