Canonical Allele Identifier: CA1059429938
Gene:

Linked Data

dbSNP Id: rs1711581068
gnomAD v3: 4-12578068-A-G
gnomAD v4: 4-12578068-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578068A>G , CM000666.2:g.12578068A>G GRCh38
NC_000004.11:g.12579692A>G , CM000666.1:g.12579692A>G GRCh37
NC_000004.10:g.12188790A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31274T>C
XR_001741374.1:n.254+44587T>C
XR_925406.3:n.140+31274T>C