Canonical Allele Identifier: CA440676079
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463837A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542680A>C , CM000666.2:g.105542680A>C GRCh38
NC_000004.11:g.106463837A>C , CM000666.1:g.106463837A>C GRCh37
NC_000004.10:g.106683286A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.325T>G
XR_939039.1:n.485T>G
XR_939040.1:n.296-1204T>G
XR_001741410.1:n.340T>G
XR_001741411.1:n.816T>G
XR_001741412.1:n.340T>G
XR_001741413.1:n.340T>G
XR_001741414.1:n.340T>G
XR_939038.2:n.340T>G
XR_939040.2:n.311-1204T>G