Canonical Allele Identifier: CA688740758
Gene:

Linked Data

dbSNP Id: rs1379980415
gnomAD v3: 12-40373600-G-T
gnomAD v4: 12-40373600-G-T
MyVariant Identifiers: chr12:g.40767402G>T (hg19) chr12:g.40373600G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373600G>T , CM000674.2:g.40373600G>T GRCh38
NC_000012.11:g.40767402G>T , CM000674.1:g.40767402G>T GRCh37
NC_000012.10:g.39053669G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944868.1:n.485-18773C>A
XR_944869.1:n.485-1548C>A
XR_001749087.1:n.380-1548C>A
XR_001749088.1:n.347-1548C>A
XR_944868.2:n.485-18773C>A
XR_944869.2:n.485-1548C>A
Search 100 bp 5'
Search 100 bp 3'