Canonical Allele Identifier: CA440675971
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463798C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542641C>A , CM000666.2:g.105542641C>A GRCh38
NC_000004.11:g.106463798C>A , CM000666.1:g.106463798C>A GRCh37
NC_000004.10:g.106683247C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.364G>T
XR_939039.1:n.524G>T
XR_939040.1:n.296-1165G>T
XR_001741410.1:n.379G>T
XR_001741411.1:n.855G>T
XR_001741412.1:n.379G>T
XR_001741413.1:n.379G>T
XR_001741414.1:n.379G>T
XR_939038.2:n.379G>T
XR_939040.2:n.311-1165G>T