Canonical Allele Identifier: CA439799417

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275099T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409382T>C , CM000666.2:g.73409382T>C	GRCh38
NC_000004.11:g.74275099T>C , CM000666.1:g.74275099T>C	GRCh37
NC_000004.10:g.74493963T>C	NCBI36
NG_009291.1:g.10128T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.510T>C MANE Select	ENSP00000295897.4:p.His170=
ENST00000295897.8:c.510T>C	ENSP00000295897.4:p.His170=
ENST00000401494.7:c.165T>C	ENSP00000384695.3:p.His55=
ENST00000415165.6:c.138-2614T>C	ENSP00000401820.2:n.138-2614T>C
ENST00000441319.5:c.516T>C	ENSP00000392541.1:p.His172=
ENST00000476441.6:c.107T>C	ENSP00000423727.1:p.Ile36Thr
ENST00000503124.5:c.60T>C	ENSP00000421027.1:p.His20=
ENST00000505649.5:n.196T>C
ENST00000509063.5:c.510T>C	ENSP00000422784.1:p.His170=
ENST00000511370.1:c.43T>C
ENST00000514786.1:n.479T>C
ENST00000621085.4:c.490+20T>C	ENSP00000483421.1:n.490+20T>C
ENST00000621628.4:c.486+306T>C	ENSP00000480485.1:n.486+306T>C
NM_000477.5:c.510T>C	NP_000468.1:p.His170=
NM_000477.6:c.510T>C	NP_000468.1:p.His170=
NM_000477.7:c.510T>C MANE Select	NP_000468.1:p.His170=