Canonical Allele Identifier: CA440676016
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463815C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542658C>A , CM000666.2:g.105542658C>A GRCh38
NC_000004.11:g.106463815C>A , CM000666.1:g.106463815C>A GRCh37
NC_000004.10:g.106683264C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.347G>T
XR_939039.1:n.507G>T
XR_939040.1:n.296-1182G>T
XR_001741410.1:n.362G>T
XR_001741411.1:n.838G>T
XR_001741412.1:n.362G>T
XR_001741413.1:n.362G>T
XR_001741414.1:n.362G>T
XR_939038.2:n.362G>T
XR_939040.2:n.311-1182G>T