Canonical Allele Identifier: CA243451923

Linked Data

dbSNP Id: rs926129043

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573485C>G , CM000674.2:g.109573485C>G GRCh38
NC_000012.11:g.110011290C>G , CM000674.1:g.110011290C>G GRCh37
NC_000012.10:g.108495673C>G NCBI36
NG_007096.1:g.5013G>C
NG_007702.1:g.4791C>G , LRG_156:g.4791C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546277.6:c.-101C>G (MVK) ENSP00000438153.2:n.-101C>G
ENST00000545712.7:c.-5G>C (MMAB) MANE Select ENSP00000445920.1:n.-5G>C
ENST00000420167.6:c.-5G>C (MMAB) ENSP00000416136.2:n.-5G>C
ENST00000503497.7:c.-5G>C (MMAB) ENSP00000474881.1:n.-5G>C
ENST00000535044.1:n.145C>G (MVK)
ENST00000537236.2:c.-5G>C (MMAB) ENSP00000483818.1:n.-5G>C
ENST00000537496.5:c.-5G>C (MMAB) ENSP00000444793.1:n.-5G>C
ENST00000539335.5:c.-92C>G (MVK) ENSP00000440379.1:n.-92C>G
ENST00000540016.5:c.-5G>C (MMAB) ENSP00000474582.1:n.-5G>C
ENST00000542390.5:n.23G>C (MMAB)
ENST00000544051.5:c.-5G>C (MMAB) ENSP00000438079.1:n.-5G>C
ENST00000545712.6:c.-5G>C (MMAB) ENSP00000445920.1:n.-5G>C
ENST00000546277.5:c.-101C>G (MVK) ENSP00000438153.1:n.-101C>G
NM_052845.3:c.-5G>C (MMAB) NP_443077.1:n.-5G>C
NR_038118.1:n.69G>C (MMAB)
XM_011538372.1:c.-101C>G (MVK) XP_011536674.1:n.-101C>G
XM_024448961.1:c.-5G>C (MMAB) XP_024304729.1:n.-5G>C
XM_024448982.1:c.-101C>G (MVK) XP_024304750.1:n.-101C>G
NM_052845.4:c.-5G>C (MMAB) MANE Select NP_443077.1:n.-5G>C
NR_038118.2:n.20G>C (MMAB)