Canonical Allele Identifier: CA357238071

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275095G>C (hg19) ; chr4:g.73409378G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409378G>C , CM000666.2:g.73409378G>C	GRCh38
NC_000004.11:g.74275095G>C , CM000666.1:g.74275095G>C	GRCh37
NC_000004.10:g.74493959G>C	NCBI36
NG_009291.1:g.10124G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.506G>C MANE Select	ENSP00000295897.4:p.Arg169Thr
ENST00000295897.8:c.506G>C	ENSP00000295897.4:p.Arg169Thr
ENST00000401494.7:c.161G>C	ENSP00000384695.3:p.Arg54Thr
ENST00000415165.6:c.138-2618G>C	ENSP00000401820.2:n.138-2618G>C
ENST00000441319.5:c.512G>C	ENSP00000392541.1:p.Arg171Thr
ENST00000476441.6:c.103G>C	ENSP00000423727.1:p.Asp35His
ENST00000503124.5:c.56G>C	ENSP00000421027.1:p.Arg19Thr
ENST00000505649.5:n.192G>C
ENST00000509063.5:c.506G>C	ENSP00000422784.1:p.Arg169Thr
ENST00000511370.1:c.39G>C
ENST00000514786.1:n.475G>C
ENST00000621085.4:c.490+16G>C	ENSP00000483421.1:n.490+16G>C
ENST00000621628.4:c.486+302G>C	ENSP00000480485.1:n.486+302G>C
NM_000477.5:c.506G>C	NP_000468.1:p.Arg169Thr
NM_000477.6:c.506G>C	NP_000468.1:p.Arg169Thr
NM_000477.7:c.506G>C MANE Select	NP_000468.1:p.Arg169Thr