Canonical Allele Identifier: CA786695512
Gene:

Linked Data

dbSNP Id: rs1161273040
gnomAD v3: 4-12578086-G-T
gnomAD v4: 4-12578086-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578086G>T , CM000666.2:g.12578086G>T GRCh38
NC_000004.11:g.12579710G>T , CM000666.1:g.12579710G>T GRCh37
NC_000004.10:g.12188808G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31256C>A
XR_001741374.1:n.254+44569C>A
XR_925406.3:n.140+31256C>A