Canonical Allele Identifier: CA2671644303
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542553A>G , CM000666.2:g.105542553A>G GRCh38
NC_000004.11:g.106463710A>G , CM000666.1:g.106463710A>G GRCh37
NC_000004.10:g.106683159A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.452T>C
XR_939039.1:n.612T>C
XR_939040.1:n.296-1077T>C
XR_001741410.1:n.467T>C
XR_001741411.1:n.943T>C
XR_001741412.1:n.449+18T>C
XR_001741413.1:n.467T>C
XR_001741414.1:n.449+18T>C
XR_939038.2:n.467T>C
XR_939040.2:n.311-1077T>C