Canonical Allele Identifier: CA103381287
Gene:

Linked Data

dbSNP Id: rs909213523

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542540G>C , CM000666.2:g.105542540G>C GRCh38
NC_000004.11:g.106463697G>C , CM000666.1:g.106463697G>C GRCh37
NC_000004.10:g.106683146G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.465C>G
XR_939039.1:n.625C>G
XR_939040.1:n.296-1064C>G
XR_001741410.1:n.480C>G
XR_001741411.1:n.956C>G
XR_001741412.1:n.449+31C>G
XR_001741413.1:n.480C>G
XR_001741414.1:n.449+31C>G
XR_939038.2:n.480C>G
XR_939040.2:n.311-1064C>G