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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.43787961A= , CM000669.2:g.43787961A=
GRCh38
NC_000007.13:g.43827560A= , CM000669.1:g.43827560A=
GRCh37
NC_000007.12:g.43794085A=
NCBI36
NG_031876.1:g.34289A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000265523.9:c.70A=
MANE Select
ENSP00000265523.4:p.Met24=
ENST00000265523.8:c.70A=
ENSP00000265523.4:p.Met24=
ENST00000402924.5:c.70A=
ENSP00000385757.1:p.Met24=
ENST00000424330.1:c.70A=
ENSP00000412005.1:p.Met24=
ENST00000453612.1:n.94A=
NM_000712.3:c.70A=
NP_000703.2:p.Met24=
NM_001253823.1:c.70A=
NP_001240752.1:p.Met24=
XM_011515474.1:c.70A=
XP_011513776.1:p.Met24=
XR_428136.2:n.265-2203T=
XR_927212.1:n.265-2203T=
XR_927213.1:n.265-2203T=
XM_011515474.3:c.70A=
XP_011513776.1:p.Met24=
XM_017012520.2:c.70A=
XP_016868009.1:p.Met24=
XM_024446867.1:c.70A=
XP_024302635.1:p.Met24=
XR_001745190.1:n.266-2203T=
NM_000712.4:c.70A=
MANE Select
NP_000703.2:p.Met24=
NM_001253823.2:c.70A=
NP_001240752.1:p.Met24=